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A clinical study of Chinese herbal compound TJAOA101 and TJAOA102 in protecting of ovarian aging

The role of TJAOA101 and TJAOA102 Chinese herbal compound in protecting ovarian aging: a prospective and before-after study.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200005532
Enrollment
Unknown
Registered
2022-01-11
Start date
2021-09-30
Completion date
Unknown
Last updated
2023-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian aging

Interventions

1:TJAOA 101
1:TJAOA 102

Sponsors

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) The age range of patient is 18-55 years old; (2) The diagnosis of women is DOR, POI, early menopause or menopausal syndrome and wish to improve ovarian function or menopausal syndrome; (3) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) The patient is known to be allergic or unsuitable for the Chinese herbal compound; (2) Women who are pregnant and lactating; (3) Patients of POI or DOR had been menopause for more than 1 year; (4) Abnormal uterine bleeding, except ovulation disorders; (5) Women who is taking hormone drugs and has stopped taking them within 3 months; (6) The diagnosis of women is endometriosis, myadenosis, submucosal fibroids or the size of non-submucosal fibroids is more than 4 cm; (7) The nature of pelvic mass is unknown; (8) The diagnosis of women is polycystic ovary syndrome, hyperprolactinemia, hyperandrogenemia, diabetes, thyroid and adrenal dysfunction and other endocrine diseases affecting ovulation; (9) Patients with serious primary diseases such as cardiovascular, liver, kidney, lung, biliary, hematopoietic system (Hb<90g/L) and malignant tumor, and psychiatric patients; (10) Patients who are participating in other clinical trials or have participated in other clinical trials within the last month; (11) Patients who are unsuitable for the study evaluated by the investigator.

Design outcomes

Secondary

MeasureTime frame
Safety assessment;

Primary

MeasureTime frame
Menstruation recovery rate;AMH;Patient's life quality;AFC;Sex hormone;

Countries

China

Contacts

Public ContactShixuan Wang
shixuanwang@tjh.tjmu.edu.cn+86 027 83663180

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026